Canonical Allele Identifier: CA1519919377

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197574G= , CM000666.2:g.186197574G=	GRCh38
NC_000004.11:g.187118728G= , CM000666.1:g.187118728G=	GRCh37
NC_000004.10:g.187355722G=	NCBI36
NG_007965.1:g.11055G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.646G= MANE Select	ENSP00000368079.4:p.Asp216=
ENST00000378802.4:c.646G=	ENSP00000368079.4:p.Asp216=
ENST00000507209.5:n.1487G=
NM_207352.3:c.646G=	NP_997235.3:p.Asp216=
XM_005262935.2:c.646G=	XP_005262992.1:p.Asp216=
XM_006714184.2:c.250G=	XP_006714247.1:p.Asp84=
XM_005262935.4:c.646G=	XP_005262992.1:p.Asp216=
XM_017008037.1:c.250G=	XP_016863526.1:p.Asp84=
NM_207352.4:c.646G= MANE Select	NP_997235.3:p.Asp216=